Canonical Allele Identifier: CA1672929636
Gene: CCDC170 HGNC NCBI
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Genomic Alleles

HGVS Genome Assembly
NC_000006.12:g.151526920C= , CM000668.2:g.151526920C= GRCh38
NC_000006.11:g.151848055C= , CM000668.1:g.151848055C= GRCh37
NC_000006.10:g.151889748C= NCBI36
NG_021198.1:g.37881C=

Transcript Alleles

HGVS Amino-acid Change
ENST00000239374.8:c.58-9398C= MANE Select ENSP00000239374.6:n.58-9398C=
ENST00000239374.7:c.58-9398C= ENSP00000239374.6:n.58-9398C=
NM_025059.3:c.58-9398C= NP_079335.2:n.58-9398C=
NM_025059.4:c.58-9398C= MANE Select NP_079335.2:n.58-9398C=
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